A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578285



Internal ID21526750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205981700..205981839hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062240
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578285
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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